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Updated: Aug 6, 2026

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
Published on: September 26, 2016
A distribution kinetics approach for crystallization of polymer blends
Jiao Yang1, Benjamin J McCoy, Giridhar Madras
1Department of Chemical Engineering, Louisiana State University, Baton Rouge, Louisiana 70803, USA.
Abstract:
The cluster distribution approach is extended to investigate the crystallization kinetics of miscible polymer blends. Mixture effects of polymer-polymer interactions are incorporated into the diffusion coefficient. The melting temperature, activation energy of diffusion, and phase transition enthalpy also depend on the blending fraction and lead to characteristic kinetic behavior of crystallization. The influence of different blending fractions is presented through the time dependence of polymer concentration, number and size of crystals, and crystallinity (in Avrami plots). Computational results indicate how overall crystallization kinetics can be expressed approximately by the Avrami equation. The nucleation rate decreases as the blending fraction of the second polymer component increases. The investigation suggests that blending influences crystal growth rate mainly through the deposition-rate driving force and growth-rate coefficient. The model is further validated by simulating the experimental data for the crystallization of a blend of poly(vinylidenefluoride)[PVDF] and poly(vinyl acetate)[PVAc] at various blending fractions.
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